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499978

Benzo[b]thien-2-ylboronic acid

≥95%

Synonym(s):

1-Benzothiophene-2-boronic acid, Benzothiophen-2-ylboronic acid, Thianaphthene-2-boronic acid

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$648.00

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About This Item

Empirical Formula (Hill Notation):
C8H7BO2S
CAS Number:
98437-23-1
Molecular Weight:
178.02
NACRES:
NA.22
PubChem Substance ID:
24873314
UNSPSC Code:
12352103
MDL number:
MFCD01075674

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InChI

1S/C8H7BO2S/c10-9(11)8-5-6-3-1-2-4-7(6)12-8/h1-5,10-11H

SMILES string

OB(O)c1cc2ccccc2s1

InChI key

YNCYPMUJDDXIRH-UHFFFAOYSA-N

assay

≥95%

mp

256-260 °C (lit.)

Quality Level

100

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This Item
512117499943436836
Benzo[b]thien-2-ylboronic acid ≥95%

Sigma-Aldrich

499978

Benzo[b]thien-2-ylboronic acid

Benzo[b]thien-3-ylboronic acid ≥95.0%

Sigma-Aldrich

512117

Benzo[b]thien-3-ylboronic acid

2-Benzofuranylboronic acid ≥95%

Sigma-Aldrich

499943

2-Benzofuranylboronic acid

2-Thienylboronic acid ≥95.0%

Sigma-Aldrich

436836

2-Thienylboronic acid

assay

≥95%

assay

≥95.0%

assay

≥95%

assay

≥95.0%

mp

256-260 °C (lit.)

mp

225-230 °C (lit.)

mp

114-116 °C (lit.)

mp

138-140 °C (lit.)

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

200

Application

Reactant involved in:
  • PDE4 inhibitors
  • Chemoselective modification of oncolytic adenovirus
  • Synthesis of phosphorescent sensor for quantification of copper(II) ion
  • UV promoted phenanthridine syntheses
  • Preparation of CYP11B1 inhibitors for treatment of cortisol dependent diseases
  • Suzuki-Miyaura cross-coupling reactions

Other Notes

Contains varying amounts of anhydride

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302,H412

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
0000237382
0000227556
0000237382
0000227556
0000120113

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S A Adediran et al.
Archives of biochemistry and biophysics, 614, 65-71 (2017-01-01)
O-Aryloxycarbonyl hydroxamates have previously been shown to covalently inactivate serine/amine amidohydrolases such as class C β-lactamases and a N-terminal hydrolase, the proteasome. We report here reactions between O-aryloxycarbonyl hydroxamates and another N-terminal hydrolase, penicillin acylase. O-Aryloxycarbonyl hydroxamates, as non-symmetric carbonates
Hyomin Jin et al.
Dalton transactions (Cambridge, England : 2003), 48(4), 1467-1476 (2019-01-12)
2-Phenylpyridine- and 2-(benzo[b]thiophen-2-yl)pyridine-based (ppy- and btp-based) o-carboranyl (Car1 and Car2) and their B(CH3)2-C∧N-chelated (Car1B and Car2B) compounds were prepared and fully characterised by multinuclear NMR spectroscopy and elemental analysis. The solid-state structure of Car2B was determined by single-crystal X-ray diffraction
Ju Hyoung Jo et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 26(70), 16733-16754 (2020-07-07)
Herein, we report the synthesis, and photochemical and -physical properties, as well as the catalytic performance, of a series of heteroleptic IrIII photosensitizers (IrPSs), [Ir(C^N)2 (N^NAryl )]+ , possessing ancillary ligands that are varied with aryl-substituents on bipyridyl unit [C^N=(2-pyridyl)benzo[b]thiophen-3-yl
Ramona Iseppi et al.
Microbial drug resistance (Larchmont, N.Y.), 24(8), 1156-1164 (2018-02-17)
We investigated the occurrence of extended-spectrum β-lactamase (ESBL), AmpC, and carbapenemase-producing Gram-negative bacteria isolated from 160 samples of fresh vegetables (n = 80) and ready-to-eat (RTE) prepacked salads (n = 80). Phenotypic and genotypic analyses were carried out on the isolates in terms of
Alberto Venturelli et al.
Journal of medicinal chemistry, 50(23), 5644-5654 (2007-10-25)
Benzo[b]thiophene-2-ylboronic acid, 1, is a 27 nM inhibitor of the class C beta-lactamase AmpC and potentiates the activity of beta-lactam antibiotics in bacteria that express this and related enzymes. As is often true, the potency of compound 1 against the
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Suzuki-Miyaura Cross-Coupling Reagents

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